ارزیابی سیتوتوکسیک In vitro ترکیبات بیواکتیو مشتق‌شده از Talaromyces minioluteus

Asgharian, P., Pirpour Tazekand, A., Hosseini, K., Forouhandeh, H., & Ghasemnejad, T. (2022). Potential mechanisms of quercetin in cancer prevention: Focus on cellular and molecular targets. Cancer Cell International, 22, Article 266. https://doi.org/10.1186/s12935-022-02677-w

Bahi, M. S., & Mustafa Shekhany, K. A. (2023). Isolation and antifungal susceptibility of Candida spp. from pediatric patients in Kurdistan of Iraq. Kurdistan Journal of Applied Research, 8(1), 47–56. https://doi.org/10.24017/science.2023.1.5

Chen, C., Sun, W.-J., Liu, X., Wei, M., Liang, Y.-H., Wang, J., Zhu, H.-C., & Zhang, Y. (2019). Anti-inflammatory spiroaxane and drimane sesquiterpenoids from Talaromyces minioluteus (Penicillium minioluteum). Bioorganic Chemistry, 91, Article 103166. https://doi.org/10.1016/j.bioorg.2019.103166

Ebaya, M. M. A., El-Mowafy, M., Adel El-Sokkary, M. M., & Hassan, R. (2020). Purification, characterization, and biocatalytic and antibiofilm activity of a novel dextranase from Talaromyces sp. International Journal of Microbiology, 2020, Article 9198048. https://doi.org/10.1155/2020/9198048

Hashemzaei, M., Delaram, A. H., Rezaie, A., Heravi, R. E., Tabrizian, K., Taghdisi, S. M., Ekhitiari Sadeghi, S., Tsarouhas, K., Kouretas, D., Tzanakakis, G., Nikitovic, D., Anisimov, N. Y., Spandidos, D. A., Tsatsakis, A. M., & Rezaee, R. (2017). Anticancer and apoptosis-inducing effects of quercetin in vitro and in vivo. Oncology Reports, 38(2), 819–828. https://doi.org/10.3892/or.2017.5766

Kaur, A., Raja, H. A., Swenson, D. C., Agarwal, R., Deep, G., Falkinham, J. O., III, & Oberlies, N. H. (2016). Talarolutins A–D: Meroterpenoids from an endophytic fungal isolate of Talaromyces minioluteus. Phytochemistry, 126, 4–10. https://doi.org/10.1016/j.phytochem.2016.03.013

Khabiri, A., Toroghi, R., Mohammadabadi, M., & Tabatabaeizadeh, S. E. (2023). Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran. Veterinary Research Forum, 14(4), Article e221. https://doi.org/10.30466/vrf.2022.548152.3373

Kundur, S., Prayag, A., Selvakumar, P., Nguyen, H., McKee, L., Cruz, C., Srinivasan, A., Shoyele, S., & Lakshmikuttyamma, A. (2019). Synergistic anticancer action of quercetin and curcumin against triple-negative breast cancer cell lines. Journal of Cellular Physiology, 234(7), 11103–11118. https://doi.org/10.1002/jcp.27761

Lan, D., & Wu, B. (2020). Chemistry and bioactivities of secondary metabolites from the genus Talaromyces. Chemistry & Biodiversity, 17(8), Article e2000229. https://doi.org/10.1002/cbdv.202000229

Lei, L.-R., Gong, L.-Q., Jin, M.-Y., Wang, R., Liu, R., Gao, J., Liu, M.-D., Huang, L., Wang, G.-Z., Wang, D., & Deng, Y. (2022). Research advances in the structures and biological activities of secondary metabolites from Talaromyces. Frontiers in Microbiology, 13, Article 984801. https://doi.org/10.3389/fmicb.2022.984801

Lewandowska, U., Gorlach, S., Owczarek, K., Hrabec, E., & Szewczyk, K. (2014). Synergistic interactions between anticancer chemotherapeutics and phenolic compounds and anticancer synergy between polyphenols. Postępy Higieny i Medycyny Doświadczalnej, 68, 528–540. https://doi.org/10.5604/17322693.1102278

Macheleidt, J., Mattern, D. J., Fischer, J., Netzker, T., Weber, J., Schroeckh, V., Valiante, V., & Brakhage, A. A. (2016). Regulation and role of fungal secondary metabolites. Annual Review of Genetics, 50, 371–392. https://doi.org/10.1146/annurev-genet-120215-035203

Newman, D. J., & Cragg, G. M. (2016). Natural products as sources of new drugs from 1981 to 2014. Journal of Natural Products, 79(3), 629–661. https://doi.org/10.1021/acs.jnatprod.5b01055

Nicoletti, R., Salvatore, M. M., & Andolfi, A. (2018). Secondary metabolites of mangrove-associated strains of Talaromyces. Marine Drugs, 16(1), Article 12. https://doi.org/10.3390/md16010012

Pyrri, I., Visagie, C. M., Soccio, P., & Houbraken, J. (2021). Re-evaluation of the taxonomy of Talaromyces minioluteus. Journal of Fungi, 7(11), Article 993. https://doi.org/10.3390/jof7110993

Nilsson, R. H., Larsson, K.-H., Taylor, A. F. S., Bengtsson-Palme, J., Jeppesen, T. S., Schigel, D., Kennedy, P., Picard, K., Glöckner, F. O., Tedersoo, L., Saar, I., Kõljalg, U., & Abarenkov, K. (2019). The UNITE database for molecular identification of fungi: Handling dark taxa and parallel taxonomic classifications. Nucleic Acids Research, 47(D1), D259–D264. https://doi.org/10.1093/nar/gky1022

Schoch, C. L., Seifert, K. A., Huhndorf, S., Robert, V., Spouge, J. L., Levesque, C. A., Chen, W., Bolchacova, E., Voigt, K., Crous, P. W., Miller, A. N., Wingfield, M. J., Aime, M. C., Smith, M. D., Barber, D., Baschien, C., Beguin, H., Cai, L., Damm, U., ... Schindel, D. (2012). Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi. Proceedings of the National Academy of Sciences of the United States of America, 109(16), 6241–6246. https://doi.org/10.1073/pnas.1117018109

Soleimanizadeh, M., Yavari, A., & Mahmoodi, Y. (2025). Evaluation of some secondary metabolites, morphophysiological and biochemical characteristics of Calendula officinalis L. under the influence of chitosan elicitor in in vitro culture. Agricultural Biotechnology Journal, 17(2), 1–30. https://doi.org/10.22103/jab.2025.24064.1618

Tang, L., Xia, J., Chen, Z., Lin, F., Shao, Z., Wang, W., & Hong, X. (2024). Cytotoxic and antibacterial meroterpenoids isolated from the marine-derived fungus Talaromyces sp. M27416. Marine Drugs, 22(4), Article 186. https://doi.org/10.3390/md22040186

Tang, Q., Ji, F., Wang, J., Guo, L., Li, Y., & Bao, Y. (2017). Quercetin exerts synergetic anti-cancer activity with 10-hydroxy camptothecin. European Journal of Pharmaceutical Sciences, 109, 223–232. https://doi.org/10.1016/j.ejps.2017.08.013

van de Loosdrecht, A. A., Beelen, R. H. J., Ossenkoppele, G. J., Broekhoven, M. G. van, & Langenhuijsen, M. M. A. C. (1994). A tetrazolium-based colorimetric MTT assay to quantitate human monocyte mediated cytotoxicity against leukemic cells from cell lines and patients with acute myeloid leukemia. Journal of Immunological Methods, 174(1–2), 311–320. https://doi.org/10.1016/0022-1759(94)90034-5

Wadhwa, K., Kapoor, N., Kaur, H., Abu-Seer, E. A., Tariq, M., Siddiqui, S., Lone, S. A., Khan, S., ... Alghamdi, S. (2024). A comprehensive review of the diversity of fungal secondary metabolites and their emerging applications in healthcare and environment. Mycobiology, 52(6), 335–387. https://doi.org/10.1080/12298093.2024.2416736

Wang, W., Wan, X., Liu, J., Wang, J., Zhu, H., Chen, C., & Zhang, Y. (2018). Two new terpenoids from Talaromyces purpurogenus. Marine Drugs, 16(5), Article 150. https://doi.org/10.3390/md16050150

White, T. J., Bruns, T. D., Lee, S. B., & Taylor, J. W. (1990). Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In M. A. Innis, D. H. Gelfand, J. J. Sninsky, & T. J. White (Eds.), PCR protocols: A guide to methods and applications (pp. 315–322). Academic Press. https://doi.org/10.1016/B978-0-12-372180-8.50042-1

Wu, H., Wu, L., Wang, J., Zhu, Q., Lin, S., Xu, J., Zheng, C., Chen, J., Qin, X., Fang, C., Zhang, Z., Azeem, S., & Lin, W. (2016). Mixed phenolic acids mediated proliferation of pathogens Talaromyces helicus and Kosakonia sacchari in continuously monocultured Radix pseudostellariae rhizosphere soil. Frontiers in Microbiology, 7, Article 335. https://doi.org/10.3389/fmicb.2016.00335

Yilmaz, N., Visagie, C. M., Houbraken, J., Frisvad, J. C., & Samson, R. A. (2014). Polyphasic taxonomy of the genus Talaromyces. Studies in Mycology, 78, 175–341. https://doi.org/10.1016/j.simyco.2014.08.001

Zhai, M. M., Li, J., Jiang, C. X., Shi, Y.-P., Di, D.-L., Crews, P., & Wu, Q.-X. (2016). The bioactive secondary metabolites from Talaromyces species. Natural Products and Bioprospecting, 6(1), 1–24. https://doi.org/10.1007/s13659-015-0081-3

Zhang, D., Wang, X., Liu, B., Li, S., Wang, Y., Guo, T., & Sun, Y. (2023). New dipyrroloquinones from a plant-derived endophytic fungus Talaromyces sp. Molecules, 28(23), Article 7847. https://doi.org/10.3390/molecules28237847